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Role of CE in a changing healthcare Role of CE in a changing healthcare

Role of CE in a changing healthcare - PowerPoint Presentation

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Role of CE in a changing healthcare - PPT Presentation

Perspectives of Mediterranean countries Almir Badnjevic Stefano Bergamasco Lejla Gurbeta Paolo Lago Lorenzo Leogrande Mario Medvedec Nicolas Pallikarakis Christophe ID: 804875

clinical medical forum engineering medical clinical engineering forum global devices health technology fourth countries final statement biomedical european management

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Role of CE in a changing healthcare. Perspectives of Mediterranean countries

Almir Badnjevic, Stefano Bergamasco, Lejla Gurbeta, Paolo Lago, Lorenzo Leogrande, Mario Medvedec, Nicolas Pallikarakis, Christophe Parret, Dusan Perovic, Ledina Picari, Jose Domingo Sanmartin

Fourth WHO Global Forum on Medical Devices

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BackgroundThanks to IFMBE and the Clinical Engineering Division we have many new opportunities to collaborate and share experiences across Clinical engineers worldwide

International events take place regularly (e.g. the ICEHTMC: Hangzhou 2015, Sao Paulo 2017, Rome 2019)Local meetings can be arranged to share experiences and common issues for specific geographical areasEuropean countries share a common legal framework (EU Directives on Medical Devices and Health Technology Assessment) that is becoming increasingly uniform with the new EU Regulations on MDs and IVDsFourth WHO Global Forum on Medical Devices2

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The event: I Forum of Clinical Engineering in the MediterraneanThe I Forum of Clinical Engineering (CE) in the Mediterranean took place in Bari, Italy the 13th of September 2018.

The event was organized by the Italian Clinical Engineers Association with the support of the Clinical Engineering Division (CED) of the International Federation for Medical and Biological Engineering (IFMBE).It gathered together representatives from 8 Mediterranean countries, either European Union (EU) members or candidate EU membersFourth WHO Global Forum on Medical Devices3

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The event: I Forum of Clinical Engineering in the MediterraneanFourth WHO Global Forum on Medical Devices

4Participants:

SpainFrance

ItalyCroatiaBosnia and HerzegovinaMontenegro

Albania

Greece

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The event: I Forum of Clinical Engineering in the MediterraneanJose Domingo

Sanmartin - Sociedad Espanola de Electromedicina e Ingenieria Clinica (SEEIC), SpainChristophe Parret - Association Francaise des Ingenieurs Biomedicaux (AFIB), FrancePaolo Lago, Stefano Bergamasco, Lorenzo Leogrande - Associazione Italiana Ingegneri Clinici

(AIIC), ItalyMario Medvedec - Croatian Biomedical Engineering and Medical Physics Society (CROBEMPS),

CroatiaLejla Gurbeta,

Almir

Badnjevic

- Bosnia and Herzegovina Medical and Biological Engineering Society (DMBIUBIH),

Bosnia and Herzegovina

Dusan

Perovic - Clinical Centre of Montenegro,

Montenegro

Ledina

Picari

– Ministry of Health,

Albania

Nicolas

Pallikarakis

- Hellenic Society of Biomedical Technology (ELEVIT), Greece

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The event: I Forum of Clinical Engineering in the Mediterranean

Left to right: Christophe Parret, Paolo Lago, Ledina Picari, Lorenzo Leogrande, Stefano Bergamasco, Mario Medvedec, Lejla Gurbeta, Dusan Perovic, Nicolas PallikarakisFourth WHO Global Forum on Medical Devices

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The Final Statement for the Global Clinical Engineering Day, 21st October 2018

A “Final statement” was prepared following the discussion during the ForumFourth WHO Global Forum on Medical Devices7

With the occasion of the Global Clinical Engineering Day, 21st October 2018, the participants want to share with the global clinical engineering community, the healthcare authorities and the public the following points that emerged as the most important for effective and safe health technology management.

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The Final Statement

Medical technology is reshaping the way health care is delivered but is at the same time becoming more complex and extremely diverse.Therefore, it requires special skills to create, deploy, regulate, assess, manage, use and maintain it, to provide quality, safety and efficiency for the benefit of patients and society in our different countries.Comprehensive knowledge and application of the regulations for market surveillance and vigilance, as well as the use of Health Technology Assessment and Health Technology Management Systems becomes more critical than ever.

The role of Clinical engineering is worldwide recognized as essential in order to cope successfully with these developments and the forthcoming challenges.

Fourth WHO Global Forum on Medical Devices

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The Final Statement (cont.)

The World Health Organization (WHO) initiative to identify an international classification, coding and nomenclature system of Medical Devices (ICMD), freely available and appropriately maintained, is of high importance.Nomenclature is the basis of a correct medical device (MD) inventory and essential for the Computerised Maintenance Management Systems, used today in all developed countries.It is also indispensable for an effective vigilance, pre- and post- market surveillance, as well as for Health Technology Assessment.

Fourth WHO Global Forum on Medical Devices

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The Final Statement (cont.)The

new EU regulations on Medical Devices 745/2017 and 746/2017 will be fully enforced in the next couple of years (May 2020 and May 2022 respectively), and all parties involved, amongst them clinical engineers, must get ready to apply them effectively. This will require dissemination of knowledge on these novel aspects, training, etc.However, many practical aspects of these regulations must still be defined by the EU commission with further acts (e.g. the MD nomenclature, UDI system, Eudamed database, single use MD reprocessing rules, etc.).The Clinical engineering professionals are very concerned about whether all these aspects will be ready and well defined in time, to avoid having "grey areas" that may lead to different and uncertain applications across countries, with different situations in terms of health technology manufacturing, post-market surveillance, management, and assessment. Cross-country collaboration will be very useful to share experiences, best practices and promote common approaches.

Fourth WHO Global Forum on Medical Devices

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The Final Statement (cont.)

Clinical engineers are key health professionals for patient care quality, safety and efficiency, and in European countries must have career paths fully regulated and contained in the European Commission Database of Regulated Professions, with career opportunities (internship, university (post)graduate specialist study, specialization/residency, sub-specialization, lifelong learning/continuing professional development) just like other health professionals with educational level 6-8.The recent effort led by the WHO to complete a global survey on the number of clinical and biomedical engineering practitioners (more than 800.000 worldwide) is extremely important for the recognition of the profession by the ILO (International Labour

Organization) as a distinct and well-defined category.Additionally, the initiative of the

European Alliance of Medical and Biological Engineering (EAMBES) that led to the creation of a European Parliament Interest Group - EPIG- on Biomedical Engineering

, is highly

recognised

as a very significant step towards the recognition of the important role of biomedical/clinical engineering in healthcare today.

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The Final Statement (cont.)In order to provide high quality, safety and efficiency of health services, it is necessary to define

clinical/biomedical engineering staffing needs in healthcare facilities based on well-defined criteria:Number and type of medical devicesMedical proceduresPatientsHospital departments and personnelHours of users training and continuing professional developmentPopulationNumber of bedsetc.Fourth WHO Global Forum on Medical Devices

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The Final Statement (cont.)Following WHO resolutions and the recent publication of the WHO Atlas on Medical Devices,

we urge European countries to involve much more clinical and biomedical engineers in activities regarding:National policies on health technologyRegulatory agenciesNational health technology assessment unitsNational health technology management unitsNotified BodiesMedical device nomenclature systemsIntroduction of medical devices into the legal metrology for establishing traceability of measurementsMedical device incorporationInventory and maintenance in health facilities

etc.

Fourth WHO Global Forum on Medical Devices

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Collaboration and … team buildingFourth WHO Global Forum on Medical Devices

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Disclosure

The presenter declares no conflict of interest with the materials provided.Fourth WHO Global Forum on Medical Devices15Thank you very much on behalf of Stefano Bergamasco (who prepared this presentation) and the whole team